15 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Nitrile Patient Examination Gloves, Powder Free
FDA 510(k)
FDA Class 1
·General Hospital
DEPILASE TWIN YAG LASER SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
EAGLE EYE PLATINUM ST CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
ECHELON*FLEX45 ARTICULATING
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·August 23, 2011
METAGLENE SCREWS DIA 4.5X24MM
FDA Adverse Event
Injury
·DEPUY FRANCE SAS 3003895575·Product code KWS·November 3, 2014
IMPAX CV REPORTING
FDA Adverse Event
Malfunction
·AGFA HEALTHCARE CORP.·Product code LLZ·July 8, 2013
EAGLE EYE PLATINUM SHORT TIP
FDA Adverse Event
Injury
·VOLCANO CORPORATION·Product code OBJ·July 1, 2016
EAGLE EYE PLATINUM SHORT TIP; EAGLE EYE PLATINUM ST CATHETER
FDA Adverse Event
Injury
·VOLCANO CORPORATION·Product code OBJ·July 1, 2016
EAGLE EYE PLATINUM SHORT TIP; EAGLE EYE PLATINUM ST CATHETER
FDA Adverse Event
Injury
·VOLCANO CORPORATION·Product code OBJ·July 1, 2016
UNKENTERPRISE2
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code NJE·June 3, 2024
UNKENTERPRISE2
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code NJE·June 3, 2024
BD MAX¿ ENTERIC VIRAL PANEL
FDA Adverse Event
Malfunction
·GENEOHM SCIENCES CANADA, INC. (BD DIAGNOSTICS)·Product code PCH·February 23, 2024
UNKENTERPRISE2
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code NJE·June 3, 2024
UNKENTERPRISE2
FDA Adverse Event
Injury
·MEDOS INTERNATIONAL SARL·Product code NJE·June 3, 2024
Model Number L111, ESSENTIO DR SL MRI Pacemaker
FDA Enforcement
Class I
·Ongoing·Boston Scientific Corporation·October 22, 2025